Method for preparing vinyl chloride through reaction of acetylene and hydrogen chloride
A technology of acetylene hydrochlorination and hydrogen chloride, which is applied in the addition preparation of hydrogen halide, chemical instruments and methods, catalyst activation/preparation, etc., can solve the problem of no industrialization, catalyst activity stability cannot meet industrialization requirements, and catalyst catalytic reaction activity is improved. limited issues
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[0098] The following Examples 1-9 relate to the preparation of non-precious metal composite catalysts, unless otherwise specified, the main implementation steps include:
[0099] (1) subjecting the catalyst carrier to pretreatment under certain conditions to obtain a pretreated catalyst carrier;
[0100] (2) modifying the catalyst carrier treated in step (1) under certain conditions to regulate the surface groups of the carrier and improve the dispersion and fixation of the catalytically active components;
[0101] (3) preparing the catalytic active component metal salt solution in turn; the catalytic metal salt solution; the alkali metal salt solution; the rare earth metal salt solution; the coordination compound solution;
[0102] (4) mixing and impregnating the modified catalyst carrier in step (2) with each group of solutions obtained in step (3);
[0103] (5) The impregnated sample is dried and calcined to obtain a non-mercury catalyst for catalyzing the hydrochlorinatio...
Embodiment 1
[0105] (1) Weigh 10 g of 40-mesh activated carbon, pretreat it with 2N hydrochloric acid solution at 60°C for 4 hours, then wash with deionized water until pH is neutral, and then dry at 100°C for 10 hours before use.
[0106] (2) Mix the pretreated activated carbon with 2N nitric acid and ammonium chloride solution, control the mass ratio of nitrogen atom to activated carbon at 1:10, ultrasonically impregnate it at 50KHZ for 2 hours, and dry it at 110°C for 12 hours after ultrasonic impregnation. After 1 hour, it was placed in a tube furnace and calcined for 2 hours in a nitrogen atmosphere to obtain the modified activated carbon.
[0107] (3) Weigh MnCl 3 and PbCl 4 Mixture, control quality and activated carbon ratio at 1:10, add water to dissolve to obtain solution I; weigh appropriate amount of LiCl and LaCl 3 Control its mass ratio to activated carbon to 1:20, add water to dissolve to obtain solution II; weigh an appropriate amount of triethyl phosphite, control its mas...
Embodiment 2
[0111] (1) Weigh 10 g of 40-purpose activated carbon, pre-treat it with 2N nitric acid solution at 80°C for 3 hours, then wash with deionized water to neutral pH, then dry at 120°C for 5 hours for later use;
[0112] (2) Mix the pretreated activated carbon with acrylamide and ammonium sulfate solution, control the mass ratio of nitrogen and sulfur atoms to the activated carbon mass at 1:5, ultrasonically impregnate it at 70KHZ for 4 hours, and dry it at 130°C after ultrasonic impregnation. After 8 hours, it was placed in a tube furnace, and calcined under nitrogen atmosphere for 2 hours to obtain modified activated carbon;
[0113] (3) Weigh TiCl 3 and IrCl 3 Mixture, control quality and activated carbon ratio at 1:20, add water to dissolve to obtain solution I; weigh an appropriate amount of BaCl 2 and LaCl 3 Control its mass ratio to activated carbon to 1:30, add water to dissolve to obtain solution II; weigh an appropriate amount of triphenylphosphorus, control its mass ...
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